Sensient Technologies Corporation; Withdrawal of Color Additive Petition, 43093 [2013-17382]
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Federal Register / Vol. 78, No. 139 / Friday, July 19, 2013 / Proposed Rules
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Issued in Washington, DC, on July 10,
2013.
Michael P. Huerta,
Administrator, Federal Aviation
Administration.
[FR Doc. 2013–17401 Filed 7–18–13; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
the color additive regulations in 21 CFR
part 74 Listing of Color Additives
Subject to Certification to provide for
the safe use of External D&C Violet No.
2 in coloring externally applied drug
products. Sensient Technologies
Corporation has now withdrawn the
petition without prejudice to a future
filing (21 CFR 71.6(c)(2)).
Dated: July 16, 2013.
Dennis M. Keefe,
Director, Office of Food Additive Safety,
Center for Food Safety and Applied Nutrition.
[FR Doc. 2013–17382 Filed 7–18–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 172 and 182
[Docket Nos. FDA–2013–F–0700 and FDA–
2013–P–0472]
Richard C. Theuer; Filing of Food
Additive Petition and Citizen Petition
AGENCY:
Sensient Technologies Corporation;
Withdrawal of Color Additive Petition
Food and Drug Administration,
HHS.
ACTION:
Notice of withdrawal.
The Food and Drug
Administration (FDA) is announcing the
withdrawal, without prejudice to a
future filing, of a color additive petition
(CAP 8C0261) proposing that the color
additive regulations be amended to
provide for the safe use of External D&C
Violet No. 2 in coloring externally
applied drug products.
FOR FURTHER INFORMATION CONTACT:
Ellen Anderson, Center for Food Safety
and Applied Nutrition (HFS–265), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740–
3835, 240–402–1309.
SUPPLEMENTARY INFORMATION: In a notice
published in the Federal Register of
August 24, 1998 (63 FR 45073), FDA
announced that a color additive petition
(CAP 8C0261) had been filed by WarnerJenkinson Co., Inc. (now part of
Sensient Cosmetic Technologies, a unit
of Sensient Technologies Corporation),
107 Wade Ave., South Plainfield, NJ
07080. The petition proposed to amend
SUMMARY:
PO 00000
Frm 00003
Fmt 4702
Notice of petition.
The Food and Drug
Administration (FDA or we) is
announcing that Richard C. Theuer,
Ph.D., has filed a petition proposing that
the food additive regulations be
amended to prohibit the use of
carrageenan and salts of carrageenan in
infant formula. In addition, the
petitioner has submitted a citizen
petition, under FDA regulations,
requesting that we amend the generally
recognized as safe (GRAS) regulations to
prohibit the use of Chondrus extract
(carrageenin) in infant formula.
FOR FURTHER INFORMATION CONTACT:
Molly A. Harry, Center for Food Safety
and Applied Nutrition (HFS–265), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740–
3835, 240–402–1075.
SUPPLEMENTARY INFORMATION: Under
section 409(b)(5) of the Federal Food,
Drug, and Cosmetic Act (the FD&C Act)
(21 U.S.C. 348(b)(5)), we are giving
notice that Richard C. Theuer, Ph.D.,
7904 Sutterton Ct., Raleigh, NC 27615,
has filed a food additive petition (FAP
3A4798; Docket No. FDA–2013–F–
0700). The petition proposes to amend
the food additive regulations in 21 CFR
172.620 and 172.626 to prohibit the use
of carrageenan and salts of carrageenan
in infant formula. In addition, Dr.
Theuer has submitted a citizen petition,
under 21 CFR 10.30, requesting that 21
SUMMARY:
[Docket No. FDA–1998–C–0381] (Formerly
Docket No. 98C–0676)
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
21 CFR Part 74
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43093
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[Federal Register Volume 78, Number 139 (Friday, July 19, 2013)]
[Proposed Rules]
[Page 43093]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-17382]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 74
[Docket No. FDA-1998-C-0381] (Formerly Docket No. 98C-0676)
Sensient Technologies Corporation; Withdrawal of Color Additive
Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice of withdrawal.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing the
withdrawal, without prejudice to a future filing, of a color additive
petition (CAP 8C0261) proposing that the color additive regulations be
amended to provide for the safe use of External D&C Violet No. 2 in
coloring externally applied drug products.
FOR FURTHER INFORMATION CONTACT: Ellen Anderson, Center for Food Safety
and Applied Nutrition (HFS-265), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740-3835, 240-402-1309.
SUPPLEMENTARY INFORMATION: In a notice published in the Federal
Register of August 24, 1998 (63 FR 45073), FDA announced that a color
additive petition (CAP 8C0261) had been filed by Warner-Jenkinson Co.,
Inc. (now part of Sensient Cosmetic Technologies, a unit of Sensient
Technologies Corporation), 107 Wade Ave., South Plainfield, NJ 07080.
The petition proposed to amend the color additive regulations in 21 CFR
part 74 Listing of Color Additives Subject to Certification to provide
for the safe use of External D&C Violet No. 2 in coloring externally
applied drug products. Sensient Technologies Corporation has now
withdrawn the petition without prejudice to a future filing (21 CFR
71.6(c)(2)).
Dated: July 16, 2013.
Dennis M. Keefe,
Director, Office of Food Additive Safety, Center for Food Safety and
Applied Nutrition.
[FR Doc. 2013-17382 Filed 7-18-13; 8:45 am]
BILLING CODE 4160-01-P
